Evidence map›Paper›PMID 24349111›Full record

ArticlePloS one2013

Metarhizium anisopliae pathogenesis of mosquito larvae: a verdict of accidental death.

Tariq M Butt, Bethany P J Greenfield, Carolyn Greig, Thierry G G Maffeis, James W D Taylor, Justyna Piasecka, Ed Dudley, Ahmed Abdulla, Ivan M Dubovskiy, Inmaculada Garrido-Jurado and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Visualizing Oral Infection Dynamics ofJournal of fungi (Basel, Switzerland) · 2025
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  12. Review
  13. Article
  14. Plants (Basel, Switzerland) · 2023
    Article
  15. Review
  16. The Potential ofJournal of fungi (Basel, Switzerland) · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 3 countries.

Tariq M ButtCollege of Science, Swansea University, Swansea, United Kingdom.
Bethany P J GreenfieldCollege of Science, Swansea University, Swansea, United Kingdom.
Carolyn GreigCollege of Science, Swansea University, Swansea, United Kingdom.
Thierry G G MaffeisCollege of Engineering, Swansea University, Swansea, United Kingdom.
James W D TaylorCollege of Science, Swansea University, Swansea, United Kingdom.
Justyna PiaseckaCollege of Science, Swansea University, Swansea, United Kingdom.
Ed DudleyCollege of Medicine, Swansea University, Swansea, United Kingdom.
Ahmed AbdullaCollege of Science, Swansea University, Swansea, United Kingdom.
Ivan M DubovskiyInstitute of Systematics and Ecology of Animals, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia.
Inmaculada Garrido-JuradoDepartment of Agricultural and Forestry Sciences, University of Cordoba, Cordoba, Spain.
Enrique Quesada-MoragaDepartment of Agricultural and Forestry Sciences, University of Cordoba, Cordoba, Spain.
Mark W PennyCollege of Engineering, Swansea University, Swansea, United Kingdom.
Daniel C EastwoodCollege of Science, Swansea University, Swansea, United Kingdom.
Swansea University · GBUniversity of Córdoba · ESInstitute of Systematics and Ecology of Animals · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metarhizium anisopliae, a fungal pathogen of terrestrial arthropods, kills the aquatic larvae of Aedes aegypti, the vector of dengue and yellow fever. The fungus kills without adhering to the host cuticle. Ingested conidia also fail to germinate and are expelled in fecal pellets. This study investigates the mechanism by which this fungus adapted to terrestrial hosts kills aquatic mosquito larvae. Genes associated with the M. anisopliae early pathogenic response (proteinases Pr1 and Pr2, and adhesins, Mad1 and Mad2) are upregulated in the presence of larvae, but the established infection process observed in terrestrial hosts does not progress and insecticidal destruxins were not detected. Protease inhibitors reduce larval mortality indicating the importance of proteases in the host interaction. The Ae. aegypti immune response to M. anisopliae appears limited, whilst the oxidative stress response gene encoding for thiol peroxidase is upregulated. Cecropin and Hsp70 genes are downregulated as larval death occurs, and insect mortality appears to be linked to autolysis through caspase activity regulated by Hsp70 and inhibited, in infected larvae, by protease inhibitors. Evidence is presented that a traditional host-pathogen response does not occur as the species have not evolved to interact. M. anisopliae retains pre-formed pathogenic determinants which mediate host mortality, but unlike true aquatic fungal pathogens, does not recognise and colonise the larval host.

Indexed as

AedesAnimalsCaspasesCecropinsFungal ProteinsGene Expression RegulationHost-Pathogen InteractionsHSP70 Heat-Shock ProteinsInsect ProteinsLarvaMetarhiziumPeroxidasesProtease InhibitorsSerine EndopeptidasesSpores, FungalVirulenceCaspasesCecropinsFungal ProteinsHSP70 Heat-Shock ProteinsInsect ProteinsPeroxidasespr1 protein, Metarhizium anisopliaeProtease InhibitorsSerine Endopeptidases

Identifiers

PMID24349111
PMCPMC3862491
OpenAlexW2162612771

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.